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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225934Generated: November 2, 2026

3-Methoxy-2-MethylBenzoic Acid → Methoxyfenozide

https://huagongshe.com/reaction/2225934

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methoxy-2-MethylBenzoic AcidHCID 7021483—
ReactantN-tert-Butyl-3,5-dimethylbenzohydrazideHCID 10878689—
SolventDichloromethaneHCID 6344—
SolventThionyl ChlorideHCID 24386—
ProductMethoxyfenozideHCID 10501064.1%

Reaction Steps

A solution of 3-methoxy-2-methylbenzoic acid (1.5 g, 0.01 tool) in thionyl chloride (10 mL) was refluxed for 45 minutes and then stripped under reduced pressure. The residue was dissolved in methylene chloride (50 mL) and added dropwise with cooling at 0° C. to a solution of N-(3,5-dimethylbenzoyl)-N-tertbutylhydrazine (4.4 g. 0.02 mol) in methylene chloride (50 mL). Following the addition, the solution was stirred overnight at room temperature and filtered. The filter-cake was washed extensively with water and ether, and then dried in vacuo to give 2.1 g (64.1% yield) of N-(3-methoxy-2-methylbenzoyl)-N'(3,5-dimethylbenzoyl)-N'-tert-butylhydrazine, melting at 204-204.5° C. 1H-NMR δppm 1.50 (s, 9H, tert-Bu), 1.63 (s, 3H, Ar-CH3), 2.25 (s, 6H, di-CH3) 3.75 (s, 6.26 (d, 1H, Ar), 6.93-7.20 (m, 5H, Ar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344958
Source datasetuspto-grants-1994_09
ORD IDord-daa008ce972e49a0905a80221bf3be18
Source noteuspto-grants-1994_09